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Remote Medical Device Engineer Jobs in Oregon (NOW HIRING)

Portalnd, Oregon - with 75% overnight travel Under remote supervision, Advanced Sterilization ... Preferred Qualifications: * 4+ years of work experience in a related Medical Device industry.

... medical device industry. * High degree of technical proficiency, excellent structured problem ... Experience with remote support systems. * Excellent communication and interpersonal skills.

FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... Paid Time Off *#LI-Remote In the event that COVID-19 vaccine mandates issued by the federal ...

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

... Medical Device regulations and standards including US-FDA, Health Canada, and the European Union ... Fully remote is not an option due to manufacturing facility-based activities. Education and ...

Salary Minimum: $66,000 Salary Maximum: $90,000 Arthrex, Inc. is a global medical device company ... This position is a remote opportunity. Duties and Responsibilities: * Design and develop engaging ...

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Biomedical Engineering Tutor

OR · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Partner with engineering teams to implement security testing practices, including SAST, DAST, SCA ... Demonstrated experience supporting or leading cybersecurity activities for medical device or other ...

Position Overview The Technical Support Engineer, MI provides remote technical support for HCUS ... FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ...

Position Overview The Technical Support Engineer, MI provides remote technical support for HCUS ... FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ...

FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... Occasional (up to 10%) travel may be required based on business need. *#LI-Remote In the event that ...

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Remote Medical Device Engineer information

See Oregon salary details

$22

$52

$102

How much do remote medical device engineer jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for remote medical device engineer in Oregon is $52.69, according to ZipRecruiter salary data. Most workers in this role earn between $37.12 and $63.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a remote medical device engineer?

To thrive as a Remote Medical Device Engineer, you need a solid background in biomedical engineering or related fields, along with experience in product development, regulatory compliance, and device testing. Familiarity with CAD software, FDA regulations (such as 21 CFR Part 820), and risk management systems is typically required, and certifications like PMP or Six Sigma can be advantageous. Strong problem-solving abilities, effective remote communication skills, and the ability to collaborate across distributed teams are crucial soft skills. These qualifications ensure that engineers can design safe, compliant devices and contribute effectively to remote, cross-functional teams.

What is a typical workday like for a remote medical device engineer?

A typical workday as a Remote Medical Device Engineer often involves designing and reviewing device components using CAD software, participating in virtual meetings to coordinate with R&D, quality assurance, and regulatory teams, and conducting documentation for regulatory submissions. You may also troubleshoot technical issues, analyze test data, and provide design updates based on feedback or test results. Regular communication with colleagues across different time zones is common, requiring flexibility and excellent organizational skills. The remote nature of the role typically offers autonomy and flexibility while maintaining close collaboration with diverse, cross-functional teams to ensure projects progress smoothly.

What is a remote medical device engineer?

A Remote Medical Device Engineer designs, develops, and tests medical devices while working from a remote location. They ensure compliance with industry regulations and collaborate with cross-functional teams to improve device functionality and safety. Responsibilities may include CAD modeling, prototyping, software integration, and regulatory documentation. Remote engineers use digital tools to communicate with teams and manage development processes efficiently. Strong technical expertise and knowledge of medical device regulations are essential for this role.

What cities in Oregon are hiring for Remote Medical Device Engineer jobs? Cities in Oregon with the most Remote Medical Device Engineer job openings:

Research Fellow, Medical Device Toxicologist

Bausch + Lomb

OR • On-site, Remote

$150K - $200K/yr

Full-time

Medical, Retirement, PTO

Re-posted 15 hours ago


Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

25th of 536 rated manufacturers


Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
The Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical device expertise supporting internal and external stakeholders pertaining to biocompatibility and associated focus areas, for medical device development, product expansion and maintenance. The Research Fellow - Medical Device Toxicologist is responsible for professional, first-line impression of the department within and outside the company through effective interactions via written and oral communications.
Responsibilities:
  • Manage team responsible for medical device biocompatibility support
  • Responsible for project strategies, risk assessments, biocompatibility evaluation plans and reports for medical devices
  • Ensures that development and execution of nonclinical strategies are aligned with product development and life cycle management activities, and with key regulatory expectations and milestones
  • Ensures that essential nonclinical data are obtained, and effectively presented for successful clinical development, regulatory and quality compliance, market launch, and maintenance of business
  • Coaches and mentors junior staff
  • Deep understanding of medical device relevant standards staying abreast of changes to applicable industry practice and guidance documents
  • Implement new and revised standards into product development projects and/or assess impact on existing products as appropriate
  • Authors and reviews department's technical documents as needed
  • Manage interactions with other functions (e.g., Product Development, Clinical Development, Analytical Chemistry, Regulatory, Quality, Compliance)
  • Liaise with company international offices on nonclinical safety matters for country-specific submissions/registrations and maintenance of business activities
  • Development and maintenance of department best practices and processes

Requirements:
  • Ph.D. in Toxicology or related discipline
  • 12+ years of relevant Medical Device industry experience
  • Experience managing a team
  • DABT preferred
  • Ophthalmic medical device experience a plus

This position may be available in the following location(s): Remote
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
For U.S. locations that require disclosure of compensation, the starting pay for this role is between $150,000.00 and $200,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.
What We Offer:
  • Comprehensive health, wellness, and retirement benefits.
  • Paid time off and programs that support work-life balance.
  • Opportunities to learn, grow, and contribute to meaningful work.

Check out our US benefits here - Employee Benefits: Bausch + Lomb
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853